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Yasuhiro Takeshima

Showing results (91-100 of 317) with videos related to

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Journal of Neuromuscular Diseases|April 12, 2024
The Association Between Physical Activity/Heart Rate Variability Data Obtained Using a Wearable Device and Timed Motor Functional Tests in Patients with Duchenne Muscular Dystrophy: A Pilot StudyAkinori Nakamura, Tsuyoshi Matsumura, Yasuhiro Takeshima, et al.
Human Genome Variation|January 5, 2024
A novel DLG4 variant causes DLG4-related synaptopathy with intellectual regressionSachi Tokunaga, Hideki Shimomura, Naoko Taniguchi, et al.
Children (Basel, Switzerland)|August 27, 2021
Views of the General Population on Newborn Screening for Spinal Muscular Atrophy in JapanTomoko Lee, Sachi Tokunaga, Naoko Taniguchi, et al.
Clinical and Experimental Nephrology|June 5, 2015
Epidemiological survey and clinical investigation of pediatric IgA nephropathyTakayuki Shibano, Nobuaki Takagi, Kohei Maekawa, et al.
Human Genome Variation|May 3, 2019
Two closely spaced mutations <i>in cis</i> result in Ullrich congenital muscular dystrophyHideki Shimomura, Tomoko Lee, Yasuhiko Tanaka, et al.
Journal of Biochemistry|November 28, 2007
A strong exonic splicing enhancer in dystrophin exon 19 achieve proper splicing without an upstream polypyrimidine tractYasuaki Habara, Mari Doshita, Sadako Hirozawa, et al.
Neuroscience Research|April 2, 2015
Glycine plays a crucial role as a co-agonist of NMDA receptors in the neuronal circuit generating body movements in rat fetusesHideki Shimomura, Mari Ito, Ayae Nishiyama, et al.
Environmental Health and Preventive Medicine|July 17, 2024
Exposure to ambient fine particulate matter components during pregnancy and early childhood and its association with asthma, allergies, and sensitization in school-age childrenKazue Ojima, Yoshiko Yoda, Shin Araki, et al.
Journal of Human Genetics|November 15, 2013
Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patientsTomoko Lee, Yasuhiro Takeshima, Noriko Kusunoki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 19, 2013
Childhood-onset hereditary pancreatitis with mutations in the CT gene and SPINK1 geneHiroyuki Awano, Tomoko Lee, Mariko Yagi, et al.
Pageof 32

Showing results (91-100 of 317) with videos related to

Sort By:
Pageof 32
Journal of Neuromuscular Diseases|April 12, 2024
The Association Between Physical Activity/Heart Rate Variability Data Obtained Using a Wearable Device and Timed Motor Functional Tests in Patients with Duchenne Muscular Dystrophy: A Pilot StudyAkinori Nakamura, Tsuyoshi Matsumura, Yasuhiro Takeshima, et al.
Human Genome Variation|January 5, 2024
A novel DLG4 variant causes DLG4-related synaptopathy with intellectual regressionSachi Tokunaga, Hideki Shimomura, Naoko Taniguchi, et al.
Children (Basel, Switzerland)|August 27, 2021
Views of the General Population on Newborn Screening for Spinal Muscular Atrophy in JapanTomoko Lee, Sachi Tokunaga, Naoko Taniguchi, et al.
Clinical and Experimental Nephrology|June 5, 2015
Epidemiological survey and clinical investigation of pediatric IgA nephropathyTakayuki Shibano, Nobuaki Takagi, Kohei Maekawa, et al.
Human Genome Variation|May 3, 2019
Two closely spaced mutations <i>in cis</i> result in Ullrich congenital muscular dystrophyHideki Shimomura, Tomoko Lee, Yasuhiko Tanaka, et al.
Journal of Biochemistry|November 28, 2007
A strong exonic splicing enhancer in dystrophin exon 19 achieve proper splicing without an upstream polypyrimidine tractYasuaki Habara, Mari Doshita, Sadako Hirozawa, et al.
Neuroscience Research|April 2, 2015
Glycine plays a crucial role as a co-agonist of NMDA receptors in the neuronal circuit generating body movements in rat fetusesHideki Shimomura, Mari Ito, Ayae Nishiyama, et al.
Environmental Health and Preventive Medicine|July 17, 2024
Exposure to ambient fine particulate matter components during pregnancy and early childhood and its association with asthma, allergies, and sensitization in school-age childrenKazue Ojima, Yoshiko Yoda, Shin Araki, et al.
Journal of Human Genetics|November 15, 2013
Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patientsTomoko Lee, Yasuhiro Takeshima, Noriko Kusunoki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 19, 2013
Childhood-onset hereditary pancreatitis with mutations in the CT gene and SPINK1 geneHiroyuki Awano, Tomoko Lee, Mariko Yagi, et al.
Pageof 32